Polymer materials

ABSTRACT

Oriented polymer material of high Young&#39;s modulus and low creep strain is provided by a process which comprises drawing polymer material having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5 at temperatures from 95 DEG C. to 140 DEG  C. and at a rate such that the deformation ratio is greater than 18.

This is a continuation of application Ser. No. 739,074, filed Nov. 5, 1976, now abandoned.

This invention relates to polymer materials and to processes for their production.

Complete Pat. No. 10746/73 describes and claims an oriented high density polyethylene polymer material having a weight average molecular weight of less than 200,000, a number average molecular weight of less than 20,000, a ratio of weight average molecular weight M_(w) to number average molecular weight M_(n) such that for M_(n) >10⁴, M_(w) /M_(n) <8 and for M_(n) <10⁴, M_(w) /M_(n) <20, and a Young's modulus as therein defined greater than 3×10¹⁰ N/m². Complete Pat. Nos. 46141/73 and 9796/74 describe and claim a process for the production of a high modulus polymer material which comprises subjecting a crystallisable polymer having a weight average molecular weight of less than 300,000 and preferably less than 200,000 to a thermal treatment such that the possibility that a given molecular chain is incorporated in more than one crystal lamella is substantially reduced, and attenuating the polymer at a temperature and a rate such that the deformation ratio is at least 15. Polymers produced according to Complete Pat. No. 10746/73 and Complete Pat. Nos. 46141/73 and 9796/74 have Young's moduli far in excess of conventional materials, but at least insofar as high density polyethylene is concerned, an improvement in creep properties would be desirable, for example for use in fibre-reinforced polymer resins and cement applications.

Surprisingly, it has now been found that the previous limitation on weight average molecular weight can be substantially exceeded if the appropriate processing conditions are employed, while still obtaining polymer materials of high modulus, and that these materials have greatly improved creep properties as is the case when these processing conditions are employed on polymer materials of lower weight average molecular weight.

According, therefore, to one aspect of the present invention there is provided an oriented polymer material having a weight average molecular weight greater than 300,000; a ratio of weight average molecular weight to number average molecular weight greater than 5, preferably greater than 9, and a Young's modulus (as hereinafter defined) greater than 3×10¹⁰ N/m².

According to a further aspect of the present invention, there is provided an oriented polymer material having a weight average molecular weight from 150,000 to 300,000; a ratio of weight average molecular weight to number average molecular weight greater than 5, preferably greater than 9; a Young's modulus (as hereinafter defined) greater than 3×10¹⁰ N/m². and a creep strain at room temperature of less than 3% after 15 hours under a stress which produces an initial strain of 1% after 10 seconds.

This invention also provides a process for the preparation of an oriented polymer material, which process comprises subjecting a crystallisable (as hereinafter defined) or amorphous polymer having a weight average molecular weight greater than 150,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, preferably greater than 9, to attenuation at a temperature from 75° C. to 140° C. and at a rate such that the deformation ratio is greater than 18.

In this specification the Young's modulus of a polymer material, depending upon the method of measurement, is defined as being the modulus measured at 21° C. by a dead-loading creep experiment, as described by Gupta and Ward in J. Macromol. Sci. Phys. B1 373 (1967), taking the stress required to produce a strain response of 0.1% at 10 secs. The deformation ratio or draw ratio is defined either as the ratio of the final length to the initial length of the deformed polymer material or as the ratio of the cross-sectional areas before and after drawing. High density polyethylene is defined in this specification as a substantially linear homopolymer of ethylene or a copolymer of ethylene containing at least 95% by weight of ethylene, having a density from 0.91 to 1.0 gm/cm³ as measured by the method of British Standard Pat. No. 2782 (1970) method 590B on a sample prepared according to British Standard Pat. No. 3412 (1966) Appendix A and annealed according to British Standard Pat. No. 3412 (1966) Appendix B(1). A crystallisable polymer is defined herein as one that is capable of forming a crystallisable or semi-crystallisable structure on cooling from the melt.

The invention may be applied to a range of crystallisable or amorphous polymers but is particularly applicable to vinyl polymers for example linear and branched chain vinyl hydrocarbon polymers such as polyethylene, polypropylene, ethylene/propylene block copolymers and ethylene/hexene-1-copolymers. The invention may also be applied to other linear or branched chain organic polymers such as polyethylene oxide, polyacetaldehyde, polyesters such as terylene and fluorinated polymers such as polytetrafluoroethylene and polychlortrifluorethylene. Particularly good results have been obtained with high density polyethylene, such as that produced by polymerising ethylene in the presence of a transition metal catalyst.

Preferably the weight average molecular weight (M_(w)) of the polymer is greater than 200,000 but less than 2,000,000, more preferably from 310,000 to 1,000,000. The number average molecular weight (M_(n)) is preferably from 15,000 to 100,000 more preferably from 15,000 to 50,000. The average molecular weights quoted in this specification are measured by gel permeation chromatography, light scattering, or by estimation from melt viscosity data.

In the process of the present invention the polymer is attenuated at a temperature and a rate such that the deformation ratio is greater than 18 and preferably at least 20. A preferred attenuation process comprises drawing the polymer to a draw ratio of at least 20. The optimum draw temperature depends upon the molecular weight of the polymer and increases with increasing molecular weight. The polymer is preferably drawn at a temperature from 85° C. to 130° C., and most preferably from 100° C. to 120° C. As a general rule the polymers are preferably drawn at speeds in excess of 1 cm per minute, usually around 5 to 50 cm per minute, or on a draw frame at speeds from 10 to 100 meters per minute. The orientation will in most cases be uniaxial, although it is also possible with an appropriate drawing process to produce biaxially oriented polymer materials.

The invention is particularly suitable for the production of fibres, films and tapes. In particular continuous filaments and tapes may be produced by melt spinning and drawing on a draw frame. For convenience the diameter of the fibre, or the thickness of the film or tape, before drawing is preferably less than 1 mm.

In continuous processes, it has been found desirable, immediately after extrusion, to pass the polymer material into a bath maintained at an elevated temperature, for example 100° C. to 125° C.

The process of the invention is capable, for example, of producing a polyethylene polymer material having a Young's modulus (as hereinbefore defined) in excess of 3×10¹⁰ N/m² and in some cases at least 5×10¹⁰ N/m² together with outstanding creep properties namely a creep strain at room temperature of less than 3% after 15 hours under a stress which produces an initial strain of 1% ofter 10 seconds. It has been found that in some cases, notably polymer materials of lower molecular weight, creep resistance can be further improved by irradiating the polymer with a suitable source of ionising radiation.

It has also been found that subjecting a polymer material to the process of the invention, its melting point can be elevated, as shown in tabular form below.

    ______________________________________                                         Polymer     Preparation    Melting Point (°C.)                          ______________________________________                                         Rigidex 50  Isotropic, quenched                                                                           ˜131                                          (--M.sub.w = 101,450)                                                                      Draw Ratio 25                                                                  Draw Temp. 75° C.                                                                      136                                                 H020-54P    Isotropic, quenched                                                                           ˜132                                          (--M.sub.w = 312,000)                                                                      Draw Ratio 25                                                                  Draw Temp. 115° C.                                                                     140                                                 ______________________________________                                          Peak melting temperature as measured in a differential scanning                calorimeter using a heating rate of 10° C./min.                   

The following Examples illustrate the invention:

EXAMPLE 1

This example describes the production of a high density polyethylene polymer material according to the invention, and a comparison of its creep properties with a low molecular weight high density polyethylene polymer.

The materials used (Table 1) were two grades of linear polyethylene homopolymer produced by B.P. Chemicals Int. (Ltd.). For comparative purposes results are also shown for a Rigidex 50 polymer (B.P. Chemicals Int. (Ltd.) with M_(w) =101,450, M_(n) =6,180, M_(w) /M_(n) =16.4 and a melt flow index (BS Method 105 C) of 6.

Dumbbell samples with gauge dimensions 1 cm×0.2 cm were cut from 0.5 mm thick sheets compression moulded at 160° C. between copper plates. The drawing was performed in an Instron Tensile Testing machine at a constant cross-head speed of 10 cm/min for 300 secs. in air and at temperatures ranging from 75° to 125°. The draw ratio was measured from the displacement of ink-marks on the sample surface originally spaced 0.1 cm apart.

The initial moduli were determined using the method of Gupta & Ward, J. Macromol. Sci. Phys. B1 373 (1967). In the long term creep experiment the sample displacement was measured optically (cathetometer) using two reference marks on the sample surface.

The results concerning the effect of draw temperature on the maximum draw ratio obtainable are summarized in Table 2. The influence of molecular weight can be clearly seen by comparing the performance of the samples at the same draw temperature. The mechanical properties of the drawn samples are shown in Table 3; it can be noted how the R 190 grade drawn to draw ratio 20 is comparable with the H020-54 samples of much higher draw ratio (34) but lower molecular weight.

                  TABLE 1                                                          ______________________________________                                         Rheological and molecular weight characteristics of samples used                       High Load Melt                                                                 Flow Index                                                                     (ASTM D 1238                                                           Grade   Contition F) --M.sub.w                                                                               --M.sub.n                                                                             --M.sub.w /--M.sub.n                      ______________________________________                                         H020-54P                                                                               2.0          312,000  33,000 9.5                                       R 190   0.11         800,000  --     >12                                       ______________________________________                                    

                  TABLE 2                                                          ______________________________________                                         Maximum effective draw ratio as a function of draw temperature                 Draw temperature                                                                              Maximum draw ratio                                              (°C.)   H020-54P     R 190                                              ______________________________________                                          75            18           12                                                  95            24           --                                                 105            30           --                                                 115            34           20                                                 120            33           --                                                 125            40           20                                                 ______________________________________                                          Rigidex 50 fails to draw at the speed used at 115° C.             

                  TABLE 3                                                          ______________________________________                                                     Initial                                                                               Creep                                                       Polymer           modulus  Stress       Strain                                 grade   Draw ratio                                                                               (GN/m.sup.2)                                                                            (GN/m.sup.2)                                                                          Time  (%)                                    ______________________________________                                         RIGIDEX 34        70       0.15   10 sec                                                                               1                                      50                                                                                                               10.sup.3 sec                                                                         2.8                                                                      2 hrs 7.5                                                                      3 hrs failure                                H020-54P                                                                               34        63       0.15   10 sec                                                                               1                                                                        10.sup.3 sec                                                                         <1.5                                                                     2 hours                                                                              <1.5                                                                     15 hrs                                                                               2                                      R 190   20        36       0.15   10 sec                                                                               0.7                                                                      10.sup.3 sec                                                                         1.6                                                                      2 hrs <2                                                                       23 hrs                                                                               2.4                                    ______________________________________                                    

EXAMPLE 2

High density polyethylene (H020-45P a product of B.P. Chemicals Int. (U.K.) Ltd.--having M_(w) of 312,000 M_(n) of 33,000 and a melt flow index--ASTM D1238 Condition F--of 2.0) was extruded at 240° C. through a spinneret having a circular orifice of 1 mm diameter to give a filament which was passed through a bath of glycerol maintained at 120° C. before being wound up at a speed of 5 m/min. The bath service was at a distance of approx. 10 cm from the spinneret and the bath dwell time was 12 sec. The spun filament had a diameter of ˜0.7 mm.

The isotropic filament was drawn on a conventional two-roller drawing frame through a glycerol bath at 120° C. The ratio of the speeds of the feed roller to the draw ratio was 1:25 with a wind-up speed of approximately 35 m/min.

The actual draw ratio attained was 23:1 as measured from the ratio of initial to final filament cross-section.

The room temperature Young's modulus was measured from the 10 sec response in a dead-loading creep experiment at a strain level of 0.1%.

                  TABLE 4                                                          ______________________________________                                                                   Young's Modulus                                      Grade       Draw Ratio    (GN/m.sup.2)                                         ______________________________________                                         H020-54P    23            35                                                   ______________________________________                                    

EXAMPLE 3

The material used was an ethylene-hexene-1 copolymer (002-55 B.P. Chemicals Int. (U.K.) Ltd.,) with the following characeteristics:

M_(n) =16,900

M_(w) =155,000

Branches (n-butyl) per 10³ C atoms 1-1.5

MFI (BS 2782 Method 105 C)=0.15

Dumbbell samples with gauge dimensions 2 cm×0.5 were cut from a 0.5 mm thick sheet compression moulded at 160° C. between copper plates and subsequently quenched in water at room temperature. The drawing was performed in an Instron Tensile Testing machine at a constant cross-head speed of 10 cm/min, in air for ˜230 sec. and at a temperature of 95° C. The draw ratio was measured from the displacement of ink marks on the sample surface. In the long term creep experiment the sample displacement was measured using a cathetometer and two reference marks on the sample surface.

The results are summarised in Table 5. It can be seen from the Table that, for the same conditions of preparation and comparable draw ratio, copolymerization produces improvements in the creep behaviour which are substantially identical to those measured for

                  TABLE 5                                                          ______________________________________                                                      Creep                                                             Polymer  Draw      Stress            Strain                                    grade    ratio     (GN/m.sup.2)                                                                             Time    %                                         ______________________________________                                         002-55   20        0.15      10.sup.3 sec                                                                           1.2                                                                    3 hrs   1.5                                                                    15 hrs  1.5                                       R 190    20        0.15      10.sup.3 sec                                                                           1.6                                                                    3 hrs   1.7                                                                    15 hrs  1.8                                       ______________________________________                                     

We claim:
 1. A process for the preparation of an oriented polymer material comprising the steps of providing a crystallisable polypropylene homopolymer having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, and attenuating said polymer at a temperature from 95° C. to 140° C. and at a rate such that the deformation ratio is greater than 18 such that said oriented polymer material has a creep strain at room temperature of less than 3% after 15 hours under stress which produces an initial strain of 1% after 10 seconds.
 2. A process for the preparation of an oriented polymer material comprising the steps of forming by extrusion a crystallisable polypropylene homopolymer having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, passing said polymer into a bath maintained at a temperature from 110° C. to 125° C. immediately after extrusion, and attenuating said polymer at a temperature from 95° C. to 140° C. and at a rate such that the deformation ratio is greater than
 18. 3. A process for the preparation of an oriented polymer material comprising the steps of providing a crystallizable polyethylene homopolymer having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, and attentuating said polymer at a temperature from 95° C. to 140° C. and at a rate such that the deformation ratio is greater than 18 such that said oriented polymer material has a creep strain at room temperature of less than 3% after 15 hours under stress which produces an initial strain of 1% after 10 seconds.
 4. A process for the preparation of an oriented polymer material comprising the steps of forming by extrusion a crystallizable polyethylene homopolymer having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, passing said polymer into a bath maintained at a temperature from 110° C. to 125° C. immediately after extrusion, and attentuating said polymer at a temperature from 95° C. to 140° C. and at a rate such that the deformation ratio is greater than
 18. 5. A process according to claim 1, 3 or 4 wherein the attenuation is effected at a temperature from 95° C. to 130° C.
 6. A process according to claim 1, 3 or 4 wherein the attenuation is effected at a temperature from 100° C. to 120° C.
 7. A process according to claim 1, 3 or 4 wherein, immediately after extrusion, the polymer material is passed into a bath maintained at 110° C. to 125° C.
 8. An oriented polymer material prepared by the process of claim 1, 3 or 4 and having a creep strain at room temperature of less than 3% after 15 hours under a stress which produces an initial strain of 1% after 10 seconds.
 9. A process for the preparation of an oriented polymer material comprising the steps of providing a crystallizable ethylene-propylene block copolymer having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, and attentuating said polymer at a temperature from 95° C. to 140° C. and at a rate such that the deformation ratio is greater than 18 such that said oriented polymer material has a creep strain at room temperature of less than 3% after 15 hours under stress which produces an initial strain of 1% after 10 seconds.
 10. A process for the preparation of an oriented polymer material comprising the steps of forming by extrusion a crystallizable ethylene-propylene block copolymer having a weight average molecular weight greater than 300,000 and a ratio of weight average molecular weight to number average molecular weight greater than 5, passing said polymer into a bath maintained at a temperature from 110° C. to 125° C. immediately after extrusion, and attentuating said polymer at a temperature from 95° C. to 140° C. and at a rate such that the deformation ratio is greater than
 18. 11. A process according to claim 1, 2, 3, 4, 9 or 10 wherein the attenuation is effected at a temperature from 110° C. to 140° C.
 12. A process according to claim 1, 2, 3, 4, 9 or 10 wherein the attenuation is effected at a temperature from 105° C. to 140° C. 